EP3770161B1 - Composé macrocyclique di(hétéro)aryle pour inhiber l'activité de la protéine kinase - Google Patents
Composé macrocyclique di(hétéro)aryle pour inhiber l'activité de la protéine kinase Download PDFInfo
- Publication number
- EP3770161B1 EP3770161B1 EP19787700.4A EP19787700A EP3770161B1 EP 3770161 B1 EP3770161 B1 EP 3770161B1 EP 19787700 A EP19787700 A EP 19787700A EP 3770161 B1 EP3770161 B1 EP 3770161B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkylene
- compound
- cycloalkyl
- reaction
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- -1 aryl macrocyclic compound Chemical class 0.000 title description 36
- 230000002401 inhibitory effect Effects 0.000 title description 12
- 230000000694 effects Effects 0.000 title description 9
- 102000001253 Protein Kinase Human genes 0.000 title description 5
- 108060006633 protein kinase Proteins 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims description 315
- 125000000623 heterocyclic group Chemical group 0.000 claims description 202
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 138
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 110
- 229910052736 halogen Inorganic materials 0.000 claims description 88
- 150000002367 halogens Chemical class 0.000 claims description 88
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 79
- 229910052757 nitrogen Inorganic materials 0.000 claims description 67
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 60
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 60
- 125000001424 substituent group Chemical group 0.000 claims description 60
- 125000001072 heteroaryl group Chemical group 0.000 claims description 52
- 150000003839 salts Chemical class 0.000 claims description 49
- 239000012453 solvate Substances 0.000 claims description 45
- 229910052760 oxygen Inorganic materials 0.000 claims description 42
- 150000004677 hydrates Chemical class 0.000 claims description 32
- 229910052717 sulfur Inorganic materials 0.000 claims description 31
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 29
- 239000008194 pharmaceutical composition Substances 0.000 claims description 28
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 26
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 26
- 229910052799 carbon Inorganic materials 0.000 claims description 22
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 21
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 21
- 206010028980 Neoplasm Diseases 0.000 claims description 13
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- 208000025966 Neurological disease Diseases 0.000 claims description 5
- 230000004054 inflammatory process Effects 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 description 380
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 168
- 230000015572 biosynthetic process Effects 0.000 description 130
- 238000003786 synthesis reaction Methods 0.000 description 129
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 127
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 99
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 87
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 87
- 239000012074 organic phase Substances 0.000 description 73
- 239000000243 solution Substances 0.000 description 70
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 66
- 125000004429 atom Chemical group 0.000 description 64
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 60
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 52
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 48
- 239000000047 product Substances 0.000 description 47
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 42
- 239000000203 mixture Substances 0.000 description 39
- 125000003118 aryl group Chemical group 0.000 description 36
- 238000004440 column chromatography Methods 0.000 description 35
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 34
- 125000000217 alkyl group Chemical group 0.000 description 33
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- 125000005842 heteroatom Chemical group 0.000 description 29
- 239000007787 solid Substances 0.000 description 27
- 239000002904 solvent Substances 0.000 description 27
- 230000014759 maintenance of location Effects 0.000 description 26
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 24
- 239000012043 crude product Substances 0.000 description 22
- 238000000034 method Methods 0.000 description 22
- 239000003814 drug Substances 0.000 description 21
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 20
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 20
- 125000000304 alkynyl group Chemical group 0.000 description 20
- 210000004027 cell Anatomy 0.000 description 20
- 239000000706 filtrate Substances 0.000 description 20
- 238000002360 preparation method Methods 0.000 description 20
- 125000003342 alkenyl group Chemical group 0.000 description 19
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 19
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 238000005160 1H NMR spectroscopy Methods 0.000 description 17
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
- 239000004480 active ingredient Substances 0.000 description 17
- 125000004452 carbocyclyl group Chemical group 0.000 description 17
- 230000003197 catalytic effect Effects 0.000 description 17
- OOWSDKUFKGVADH-UHFFFAOYSA-N 1-diphenylphosphoryloxy-2,3,4,5,6-pentafluorobenzene Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1OP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 OOWSDKUFKGVADH-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 239000003054 catalyst Substances 0.000 description 15
- 238000001914 filtration Methods 0.000 description 15
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 14
- 239000007788 liquid Substances 0.000 description 14
- 238000011282 treatment Methods 0.000 description 14
- 239000008346 aqueous phase Substances 0.000 description 13
- 201000010099 disease Diseases 0.000 description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- 150000001721 carbon Chemical group 0.000 description 12
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 12
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 11
- 239000012071 phase Substances 0.000 description 11
- 238000000746 purification Methods 0.000 description 11
- 150000003254 radicals Chemical class 0.000 description 11
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 10
- 102100033793 ALK tyrosine kinase receptor Human genes 0.000 description 10
- 239000000945 filler Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 229940124597 therapeutic agent Drugs 0.000 description 10
- 238000000825 ultraviolet detection Methods 0.000 description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 210000004369 blood Anatomy 0.000 description 9
- 239000008280 blood Substances 0.000 description 9
- 125000000753 cycloalkyl group Chemical group 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 101000686031 Homo sapiens Proto-oncogene tyrosine-protein kinase ROS Proteins 0.000 description 8
- 108091000080 Phosphotransferase Proteins 0.000 description 8
- 102100023347 Proto-oncogene tyrosine-protein kinase ROS Human genes 0.000 description 8
- 230000002378 acidificating effect Effects 0.000 description 8
- 238000004458 analytical method Methods 0.000 description 8
- 229910002092 carbon dioxide Inorganic materials 0.000 description 8
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 8
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 8
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 8
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 8
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 8
- 102000020233 phosphotransferase Human genes 0.000 description 8
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- 229940002612 prodrug Drugs 0.000 description 8
- 238000010992 reflux Methods 0.000 description 8
- 241000700159 Rattus Species 0.000 description 7
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- 229940079593 drug Drugs 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
- 230000001225 therapeutic effect Effects 0.000 description 7
- SHAHPWSYJFYMRX-GDLCADMTSA-N (2S)-2-(4-{[(1R,2S)-2-hydroxycyclopentyl]methyl}phenyl)propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1C[C@@H]1[C@@H](O)CCC1 SHAHPWSYJFYMRX-GDLCADMTSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920000858 Cyclodextrin Polymers 0.000 description 6
- 238000006646 Dess-Martin oxidation reaction Methods 0.000 description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 6
- 125000004122 cyclic group Chemical group 0.000 description 6
- NKLCNNUWBJBICK-UHFFFAOYSA-N dess–martin periodinane Chemical compound C1=CC=C2I(OC(=O)C)(OC(C)=O)(OC(C)=O)OC(=O)C2=C1 NKLCNNUWBJBICK-UHFFFAOYSA-N 0.000 description 6
- YNHIGQDRGKUECZ-UHFFFAOYSA-N dichloropalladium;triphenylphosphanium Chemical compound Cl[Pd]Cl.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-N 0.000 description 6
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- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 6
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 6
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- VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 6
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- 208000024891 symptom Diseases 0.000 description 6
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 5
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- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
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- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
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- DAAXYQZSKBPJOX-FQEVSTJZSA-N (2S)-2-amino-3-[4-[5-[3-(4-hydroxyphenyl)-4-methoxyphenyl]-1,2,4-oxadiazol-3-yl]phenyl]propanoic acid Chemical compound COC1=C(C=C(C=C1)C2=NC(=NO2)C3=CC=C(C=C3)C[C@@H](C(=O)O)N)C4=CC=C(C=C4)O DAAXYQZSKBPJOX-FQEVSTJZSA-N 0.000 description 4
- UNSHMXUHOHBLIQ-UHFFFAOYSA-N 3-[4-chloro-3-(2-methylphenoxy)naphthalen-1-yl]-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione Chemical compound ClC1=C(C=C(C2=CC=CC=C12)N1C(NC(=CC1=O)C(F)(F)F)=O)OC1=C(C=CC=C1)C UNSHMXUHOHBLIQ-UHFFFAOYSA-N 0.000 description 4
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- 125000006163 5-membered heteroaryl group Chemical group 0.000 description 4
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
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- WDAXFOBOLVPGLV-UHFFFAOYSA-N ethyl isobutyrate Chemical compound CCOC(=O)C(C)C WDAXFOBOLVPGLV-UHFFFAOYSA-N 0.000 description 4
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- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 4
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- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 description 3
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- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
- 125000005305 thiadiazolinyl group Chemical group 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000005458 thianyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000001583 thiepanyl group Chemical group 0.000 description 1
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- 125000002053 thietanyl group Chemical group 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 229940100611 topical cream Drugs 0.000 description 1
- 229940100615 topical ointment Drugs 0.000 description 1
- 229940044693 topoisomerase inhibitor Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
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- 230000026683 transduction Effects 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000005881 triazolinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- 230000004565 tumor cell growth Effects 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 230000003827 upregulation Effects 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical class CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 229960003862 vemurafenib Drugs 0.000 description 1
- GPXBXXGIAQBQNI-UHFFFAOYSA-N vemurafenib Chemical compound CCCS(=O)(=O)NC1=CC=C(F)C(C(=O)C=2C3=CC(=CN=C3NC=2)C=2C=CC(Cl)=CC=2)=C1F GPXBXXGIAQBQNI-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
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- 229910052727 yttrium Inorganic materials 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/18—Bridged systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/529—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim forming part of bridged ring systems
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/48—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
- C07C215/50—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/18—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by doubly-bound oxygen atoms
-
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C313/00—Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C313/02—Sulfinic acids; Derivatives thereof
- C07C313/06—Sulfinamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/20—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
Definitions
- the present disclosure belongs to the technical field of medicine, and particularly relates to specific di(hetero)aryl macrocyclic compounds, pharmaceutical compositions containing them, and preparation methods thereof and use thereof for the treatment of cancers, pain, neurological diseases, autoimmune diseases and inflammation.
- Protein kinases are key regulators of cell growth, proliferation and survival. Genetic and epigenetic changes accumulate in cancer cells, leading to abnormal activation of signal transduction pathways that drive malignant processes. The inhibition of these signal transduction pathways represents a promising intervention opportunity for targeted cancer therapies.
- ALK belongs to the insulin receptor (IR) superfamily of tyrosine receptor kinases. Due to the important role of ALK in hematogenesis, solid and stromal tumors, it is considered to be an attractive molecular target for therapeutic intervention of cancers.
- IR insulin receptor
- TRK Tropomyosin-related tyrosine receptor kinase
- NT neurotrophin
- ROS1 kinase is a tyrosine receptor kinase with an unknown ligand. It has been reported that ROS 1 kinase undergoes gene rearrangement to produce constitutively active fusion proteins in many human cancers, including glioblastoma, non-small cell lung cancer (NSCLC), bile duct carcinoma, ovarian cancer, gastric adenocarcinoma, colorectal cancer, inflammatory myofibroblastic tumor, angiosarcoma and epithelioid hemangioendothelioma.
- NSCLC non-small cell lung cancer
- bile duct carcinoma ovarian cancer
- gastric adenocarcinoma gastric adenocarcinoma
- colorectal cancer colorectal cancer
- inflammatory myofibroblastic tumor angiosarcoma
- epithelioid hemangioendothelioma epithelioid hemangioendothelio
- the di(hetero)aryl macrocyclic compounds of the present disclosure can effectively bind to the ATP binding sites of ALK, ROS1, and TRK kinases, and exhibit inhibitory effect on these proteins. More importantly, the compounds can bind to mutant types of these proteins, such as ALK G1202R, ALK L1196M, ROS1 G2032R or TRKA G595R and the like. More importantly, it can bind to mutants of these proteins.
- the compounds of the present disclosure are inhibitors of wild and mutant ALK, ROS1, TRK, etc. and will be used to treat subjects with abnormal signaling of one or more of ALK, ROS1 or TRK.
- the present disclosure provides a new di(hetero)aryl macrocyclic compound and a composition containing the compound and use thereof, which has better inhibitory activity against wild and mutant ALK, ROS 1, TRK and other kinases, with lower side effects and/or better pharmacodynamics/pharmacokinetic properties, and can be used in the treatment of diseases mediated by one or more of ALK, ROS1 or TRK.
- the present disclosure provides a pharmaceutical composition
- a pharmaceutical composition comprising a compound of the present disclosure or the pharmaceutically acceptable salt, enantiomer, diastereomer, racemate, solvate, hydrate, polymorph, prodrug or active metabolite thereof and pharmaceutically acceptable excipient(s).
- the compound of the present disclosure is provided in the pharmaceutical composition in an effective amount.
- the compound of the present disclosure is provided in a therapeutically effective amount.
- the compound of the present disclosure is provided in a prophylactically effective amount.
- the present disclosure provides a pharmaceutical composition
- a pharmaceutical composition comprising a compound of the present disclosure and pharmaceutically acceptable excipient(s), which also contains other therapeutic agent(s).
- the present disclosure provides a kit comprising a compound of the present disclosure or the pharmaceutically acceptable salt, enantiomer, diastereomer, racemate, solvate, hydrate, polymorph, prodrug or active metabolite thereof, optionally other therapeutic agent(s) and pharmaceutically acceptable carrier(s), adjuvant(s) or vehicle(s).
- the present disclosure provides a method for preparing a pharmaceutical composition as described above, including the following steps: mixing pharmaceutically acceptable excipient(s) with the compound of the present disclosure or the pharmaceutically acceptable salt, enantiomer, diastereomer, racemate, solvate, hydrate, polymorph, prodrug or active metabolite thereof to form a pharmaceutical composition.
- the present disclosure provides a compound for use in a method for treating cancers, pain, neurological diseases, autoimmune diseases and inflammation in a subject in need thereof, the method includes administering to the subject an effective amount of the compound of the present disclosure or the pharmaceutically acceptable salt, enantiomer, diastereomer, racemate, solvate, hydrate, polymorph, prodrug or active metabolite thereof or the pharmaceutical composition of the present disclosure.
- the compound is administered orally, subcutaneously, intravenously or intramuscularly.
- the compound is administered chronically.
- the present disclosure relates to a compound for use in a method for inhibiting proteins or tyrosine kinases (including one or more of ALK, ROS1, and TRK), which comprises contacting one or more of the kinases with an effective amount of at least one of the compound of formula (I) or the pharmaceutically acceptable salt, enantiomer, diastereomer, racemate, solvate, hydrate, polymorph, prodrug or active metabolite thereof, and/or contacting with at least one pharmaceutical composition of the present disclosure, wherein the said contact is occurs ex vivo, in vitro or in vivo.
- proteins or tyrosine kinases including one or more of ALK, ROS1, and TRK
- C 1-6 alkyl is intended to encompass, C 1 , C 2 , C 3 , C 4 , C 5 , C 6 , C 1-6 , C 1-5 , C 1-4 , C 1-3 , C 1-2 , C 2-6 , C 2-5 , C 2-4 , C 2-3 , C 3-6 , C 3-5 , C 3-4 , C 4-6 , C 4-5 and C 5-6 alkyl.
- C 1-6 alkyl refers to a radical of a straight-chain or branched saturated hydrocarbon group having from 1 to 6 carbon atoms, and it is also referred to herein as "lower alkyl”. In some embodiments, C 1-4 alkyl is particularly preferred.
- alkyl groups include, but are not limited to, methyl (C 1 ), ethyl (C 2 ), n-propyl (C 3 ), isopropyl (C 3 ), n-butyl (C 4 ), tert-butyl (C 4 ), sec-butyl (C 4 ), iso-butyl (C 4 ), n-pentyl (C 5 ), 3-pentanyl (C 5 ), amyl (C 5 ), neopentyl (C 5 ), 3-methyl-2-butanyl (C 5 ), tertiary amyl (C 5 ), and n-hexyl (C 6 ).
- each instance of an alkyl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
- Appropriate substituents are defined below.
- C 2-6 alkenyl refers to a radical of a straight-chain or branched hydrocarbon group having from 2 to 6 carbon atoms, one or more carbon-carbon double bonds (e.g., 1, 2, or 3 carbon-carbon double bonds).
- the one or more carbon-carbon double bonds may be internal (such as in 2-butenyl) or terminal (such as in 1-butenyl).
- C 2-4 alkenyl is particularly preferred.
- alkenyl groups include, but are not limited to, ethenyl (C 2 ), 1-propenyl (C 3 ), 2-propenyl (C 3 ), 1-butenyl (C 4 ), 2-butenyl (C 4 ), butadienyl (C 4 ), pentenyl (C 5 ), pentadienyl (C 5 ), hexenyl (C 6 ), and the like.
- each instance of an alkenyl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent. Appropriate substituents are defined below.
- C 2-6 alkynyl refers to a radical of a straight-chain or branched hydrocarbon group having from 2 to 6 carbon atoms, one or more carbon-carbon triple bonds (e.g., 1, 2, or 3 carbon-carbon triple bonds), and optionally one or more carbon-carbon double bonds (e.g., 1, 2, or 3 carbon-carbon double bonds).
- C 2-4 alkynyl is particularly preferred.
- alkynyl does not contain any double bonds.
- the one or more carbon-carbon triple bonds may be internal (such as in 2-butynyl) or terminal (such as in 1-butynyl).
- alkynyl groups examples include, but are not limited to, ethynyl (C 2 ), 1-propynyl (C 3 ), 2-propynyl (C 3 ), 1-butynyl (C 4 ), 2-butynyl (C 4 ), pentynyl (C 5 ), hexynyl (C 6 ), and the like. Regardless of whether the alkynyl group is modified with "substituted", each instance of an alkynyl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent. Appropriate substituents are defined below.
- C 1-6 alkylene refers to a divalent group formed by removing another hydrogen of the C 1-6 alkyl, and can be a substituted or unsubstituted alkylene. In some embodiments, C 1-4 alkylene is particularly preferred.
- the unsubstituted alkylene groups include, but are not limited to, methylene (-CH 2 -), ethylene (-CH 2 CH 2 -), propylene (-CH 2 CH 2 CH 2 -), butylene (-CH 2 CH 2 CH 2 CH 2 -), pentylene (-CH 2 CH 2 CH 2 CH 2 CH 2 -), hexylene (-CH 2 CH 2 CH 2 CH 2 CH 2 CH 2 -), etc.
- substituted alkylene groups such as those substituted with one or more alkyl (methyl) groups, include, but are not limited to, substituted methylene (-CH(CH 3 )-, - C(CH 3 ) 2 -), substituted ethylene (-CH(CH 3 )CH 2 -, -CH 2 CH(CH 3 )-, -C(CH 3 ) 2 CH 2 -, - CH 2 C(CH 3 ) 2 -), substituted propylene (-CH(CH 3 )CH 2 CH 2 -, -CH 2 CH(CH 3 )CH 2 -, - CH 2 CH 2 CH(CH 3 )-, -C(CH 3 ) 2 CH 2 CH 2 -, -CH 2 C(CH 3 ) 2 CH 2 -, -CH 2 CH 2 C(CH 3 ) 2 -), etc.
- substituted methylene -CH(CH 3 )-, - C(CH 3 ) 2 -
- substituted ethylene -CH(CH 3
- C 0-6 alkylene includes the chemical bond and C 1-6 alkylene groups as defined above.
- C 1-6 alkoxy refers to the group -OR wherein R is a substituted or unsubstituted C 1-6 alkyl group. In some embodiments, C 1-4 alkoxy group is particularly preferred. Specific alkoxy groups include, but are not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentyloxy, n-hexyloxy and 1,2-dimethylbutoxy.
- Halo or halogen means fluorine (F), chlorine (Cl), bromine (Br) and iodine (I).
- the halo group is F, -Cl or Br.
- the halogen group is F or Cl.
- the halogen group is F.
- C 1-6 haloalkyl and “C 1-6 haloalkoxy” refer to the above “C 1-6 alkyl” and “C 1-6 alkoxy", which are substituted by one or more halo groups.
- C 1-4 haloalkyl group is particularly preferred, and more preferably C 1-2 haloalkyl group.
- C 1-4 haloalkoxy group is particularly preferred, and more preferably C 1-2 haloalkoxy group.
- Exemplary haloalkyl groups include, but are not limited to, -CF 3 , -CH 2 F, - CHF 2 , -CHFCH 2 F, -CH 2 CHF 2 , -CF 2 CF 3 , -CCl 3 , -CH 2 Cl, -CHCl 2 , 2,2,2-trifluoro-1,1-dimethylethyl, and the like.
- Exemplary haloalkoxy groups include, but are not limited to: -OCH 2 F, - OCHF 2 , -OCF 3 , and the like.
- C 3-10 cycloalkyl refers to a radical of a non-aromatic cyclic hydrocarbon group having from 3 to 10 ring carbon atoms and zero heteroatoms. In some embodiments, C 3-7 cycloalkyl is preferred, C 3-6 cycloalkyl is particularly preferred, and C 5-6 cycloalkyl is more preferred. Cycloalkyl also includes ring systems wherein the cycloalkyl ring, as defined above, is fused with one or more aryl or heteroaryl groups wherein the point of attachment is on the cycloalkyl ring, and in such instances, the number of carbons continue to designate the number of carbons in the cycloalkyl ring system.
- Exemplary cycloalkyl groups include, but is not limited to, cyclopropyl (C 3 ), cyclopropenyl (C 3 ), cyclobutyl (C 4 ), cyclobutenyl (C 4 ), cyclopentyl (C 5 ), cyclopentenyl (C 5 ), cyclohexyl (C 6 ), cyclohexenyl (C 6 ), cyclohexadienyl (C 6 ), cycloheptyl (C 7 ), cycloheptenyl (C 7 ), cycloheptadienyl (C 7 ), cycloheptatrienyl (C 7 ), cyclooctyl (C 8 ), cyclooctenyl (C 8 ), bicyclo[2.2.1]heptanyl (C 7 ), bicyclo[2.2.2]octanyl (C 8 ), cyclononyl (C 9 ), cyclononen
- each instance of a cycloalkyl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
- Appropriate substituents are defined below.
- 3- to 10-membered heterocyclyl refers to a radical of a 3- to 10-membered non-aromatic ring system having ring carbon atoms and 1 to 4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen, sulfur, boron, phosphorus, and silicon.
- the point of attachment may be a carbon or nitrogen atom, as valency permits.
- 3- to 7-membered heterocyclyl is preferred, which is a radical of a 3- to 7-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms; in some embodiments, 3- to 6-membered heterocyclyl is particularly preferred, which is a radical of a 3- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms; 5- to 6-membered heterocyclyl is more preferred, which is a radical of a 5- to 6-membered non-aromatic ring system having ring carbon atoms and 1 to 3 ring heteroatoms.
- Heterocyclyl also includes ring systems wherein the heterocyclyl ring, as defined above, is fused with one or more aryl or heteroaryl groups, wherein the point of attachment is on the heterocyclyl ring; and in such instances, the number of ring members continue to designate the number of ring members in the heterocyclyl ring system.
- each instance of an heterocyclyl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent. Appropriate substituents are defined below.
- Exemplary 3-membered heterocyclyl groups containing one heteroatom include, but are not limited to, azirdinyl, oxiranyl, thiorenyl.
- Exemplary 4-membered heterocyclyl groups containing one heteroatom include, but are not limited to, azetidinyl, oxetanyl and thietanyl.
- Exemplary 5-membered heterocyclyl groups containing one heteroatom include, but are not limited to, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothiophenyl, dihydrothiophenyl, pyrrolidinyl, dihydropyrrolyl and pyrrolyl-2,5-dione.
- Exemplary 5-membered heterocyclyl groups containing two heteroatoms include, but are not limited to, dioxolanyl, oxasulfuranyl, disulfuranyl and oxazolidin-2-one.
- Exemplary 5-membered heterocyclyl groups containing three heteroatoms include, but are not limited to, triazolinyl, oxadiazolinyl, and thiadiazolinyl.
- Exemplary 6-membered heterocyclyl groups containing one heteroatom include, but are not limited to, piperidinyl, tetrahydropyranyl, dihydropyridinyl and thianyl.
- Exemplary 6-membered heterocyclyl groups containing two heteroatoms include, but are not limited to, piperazinyl, morpholinyl, dithianyl, dioxanyl.
- Exemplary 6-membered heterocyclyl groups containing three heteroatoms include, but are not limited to, triazinanyl.
- Exemplary 7-membered heterocyclyl groups containing one heteroatom include, but are not limited to, azepanyl, oxepanyl and thiepanyl.
- Exemplary 8-membered heterocyclyl groups containing one heteroatom include, but are not limited to, azocanyl, oxecanyl and thiocanyl.
- Exemplary 5-membered heterocyclyl groups fused to a C 6 aryl ring include, but are not limited to, indolinyl, isoindolinyl, dihydrobenzofuranyl, dihydrobenzothienyl, benzoxazolinonyl, and the like.
- Exemplary 6-membered heterocyclyl groups fused to an C 6 aryl ring include, but are not limited to, tetrahydroquinolinyl, tetrahydroisoquinolinyl, and the like.
- C 6-14 aryl refers to a radical of a monocyclic or polycyclic (e.g., bicyclic or tricyclic) 4n+2 aromatic ring system ( e.g., having 6, 10, or 14 ⁇ electrons shared in a cyclic array) having 6-14 ring carbon atoms and zero heteroatoms.
- an aryl group has six ring carbon atoms ("C 6 aryl”; e.g., phenyl).
- an aryl group has ten ring carbon atoms ("C 10 aryl”; e.g., naphthyl such as 1-naphthyl and 2-naphthyl).
- an aryl group has fourteen ring carbon atoms ("C 14 aryl"; e.g., anthracyl). In some embodiments, C 6-10 aryl is particularly preferred, and C 6 aryl is more preferred.
- Aryl also includes ring systems wherein the aryl ring, as defined above, is fused with one or more cycloalkyl or heterocyclyl groups and the radical or point of attachment is on the aryl ring, and in such instances, the number of carbon atoms continue to designate the number of carbon atoms in the aryl ring system.
- each instance of an aryl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
- Appropriate substituents are defined below.
- 5- to 10-membered heteroaryl refers to a radical of a 5-10 membered monocyclic or bicyclic 4n+2 aromatic ring system ( e.g., having 6 or 10 ⁇ electrons shared in a cyclic array) having ring carbon atoms and 1-4 ring heteroatoms, wherein each heteroatom is independently selected from nitrogen, oxygen and sulfur.
- the point of attachment may be a carbon or nitrogen atom, as valency permits.
- Heteroaryl bicyclic ring systems can include one or more heteroatoms in one or both rings.
- Heteroaryl includes ring systems wherein the heteroaryl ring, as defined above, is fused with one or more cycloalkyl or heterocyclyl groups wherein the point of attachment is on the heteroaryl ring, and in such instances, the number of ring members continue to designate the number of ring members in the heteroaryl ring system.
- 5- to 6-membered heteroaryl group is particularly preferred, which is a 5-6 membered monocyclic or bicyclic 4n+2 aromatic ring system having ring carbon atoms and 1-4 ring heteroatoms.
- each instance of an heteroaryl group is independently optionally substituted, e.g., for instance with from 1 to 5 substituents, 1 to 3 substituents, or 1 substituent.
- Appropriate substituents are defined below.
- Exemplary 5-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyrrolyl, furanyl and thiophenyl.
- Exemplary 5-membered heteroaryl groups containing two heteroatoms include, but are not limited to, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, and isothiazolyl.
- Exemplary 5-membered heteroaryl groups containing three heteroatoms include, but are not limited to, triazolyl, oxadiazolyl, and thiadiazolyl.
- Exemplary 5-membered heteroaryl groups containing four heteroatoms include, but are not limited to, tetrazolyl.
- Exemplary 6-membered heteroaryl groups containing one heteroatom include, but are not limited to, pyridinyl.
- Exemplary 6-membered heteroaryl groups containing two heteroatoms include, but are not limited to, pyridazinyl, pyrimidinyl, and pyrazinyl.
- Exemplary 6-membered heteroaryl groups containing three or four heteroatoms include, but are not limited to, triazinyl and tetrazinyl, respectively.
- Exemplary 7-membered heteroaryl groups containing one heteroatom include, but are not limited to, azepinyl, oxepinyl, and thiepinyl.
- Exemplary 5,6-bicyclic heteroaryl groups include, but are not limited to, indolyl, isoindolyl, indazolyl, benzotriazolyl, benzothiophenyl, isobenzothiophenyl, benzofuranyl, benzoisofuranyl, benzimidazolyl, benzoxazolyl, benzisoxazolyl, benzoxadiazolyl, benzthiazolyl, benzisothiazolyl, benzthiadiazolyl, indolizinyl, and purinyl.
- Exemplary 6,6-bicyclic heteroaryl groups include, but are not limited to, naphthyridinyl, pteridinyl, quinolinyl, isoquinolinyl, cinnolinyl, quinoxalinyl, phthalazinyl, and quinazolinyl.
- pharmaceutically acceptable salt refers to those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, and are commensurate with a reasonable benefit/risk ratio.
- Pharmaceutically acceptable salts are well known in the art. For example, Berge et al., describes pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences (1977) 66: 1-19 .
- Pharmaceutically acceptable salts of the compounds of the present disclosure include those derived from suitable inorganic and organic acids and inorganic and organic bases.
- Examples of pharmaceutically acceptable, nontoxic acid addition salts are salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid and perchloric acid or with organic acids such as acetic acid, oxalic acid, maleic acid, tartaric acid, citric acid, succinic acid or malonic acid. Salts formed by using regular methods used in the art such as ion exchange are also included.
- salts include adipate, alginate, ascorbate, aspartate, benzenesulfonate, benzoate, bisulfate, borate, butyrate, camphorate, camphorsulfonate, citrate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptonate, glycerophosphate, gluconate, hemisulfate, heptanoate, hexanoate, hydroiodide, 2-hydroxy-ethanesulfonate, lactobionate, lactate, laurate, lauryl sulfate, malate, maleate, malonate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, nitrate, oleate, oxalate, palmitate, pamoate, pectinate,
- Pharmaceutically acceptable salts derived from appropriate bases include alkali metal, alkaline earth metal, ammonium and N + (C 1-4 alkyl) 4 salts.
- Representative alkali or alkaline earth metal salts include sodium, lithium, potassium, calcium, magnesium, and the like.
- Other pharmaceutically acceptable salts include, when appropriate, nontoxic ammonium, quaternary ammonium, and amine cations formed with counterions such as halide, hydroxide, carboxylate, sulfate, phosphate, nitrate, lower alkyl sulfonate, and aryl sulfonate.
- a "subject" to which administration is contemplated includes, but is not limited to, humans (i.e., a male or female of any age group, e.g., a pediatric subject (e.g., infant, child, adolescent) or adult subject ( e.g., young adult, middle-aged adult or senior adult)) and/or a non-human animal, e.g., a mammal such as primates (e.g., cynomolgus monkeys, rhesus monkeys), cattle, pigs, horses, sheep, goats, rodents, cats, and/or dogs.
- the subject is a human.
- the subject is a non-human animal.
- the terms "human", “patient” and “subject” are used interchangeably herein.
- the terms “treat”, “treating” and “treatment” contemplate an action that occurs while a subject is suffering from the specified disease, disorder or condition, which reduces the severity of the disease, disorder or condition, or retards or slows the progression of the disease, disorder or condition ("therapeutic treatment”), and also contemplates an action that occurs before a subject begins to suffer from the specified disease, disorder or condition (“prophylactic treatment").
- Combination and related terms mean the simultaneous or sequential administration of a therapeutic agent of the present disclosure.
- a compound disclosed herein may be administered simultaneously or sequentially with another therapeutic agent in separate unit dosage forms, or together with another therapeutic agent in a single unit dosage form.
- the compound of the present disclosure refers to the compound of formula (I) to the compound of formula (VI) and the compound of formula (I') to the compound of formula (V') (including the subsets of each formula, such as the compound of formula (III-1)), or pharmaceutically acceptable salts, enantiomers, diastereomers, racemates, solvates, hydrates, or polymorphs thereof.
- the present disclosure relates to the compound of formula (I): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (II): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (III-1) or (III-2): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (IV-1) or (IV-2): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (V-1) or (V-2): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (VI-1) or (VI-2): wherein,
- the present disclosure relates to the aforementioned compound, which is the compound of formula (I'): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (II'): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (III'-1) or (III'-2): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (IV'-1) or (IV'-2): wherein,
- the present disclosure relates to the aforementioned compound, which is of formula (V'-1) or (V'-2): wherein,
- a 1 is CR 1 ; in another specific embodiment, A 1 is CH; in another specific embodiment, A 1 is N.
- a 2 is CR 2 ; in another specific embodiment, A 2 is CH; in another specific embodiment, A 2 is N.
- a 3 is CR 3 ; in another specific embodiment, A 3 is CH; in another specific embodiment, A 3 is CF; in another specific embodiment, A 3 is N.
- a 4 is CR 4 ; in another specific embodiment, A 4 is CH; in another specific embodiment, A 4 is N.
- R 1 , R 2 , R 3 and R 4 are independently H; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently halogen; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -CN; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -NO 2 ; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently - OR a ; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -SR a ; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -NR b R c ; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -C(O)R a ; in another specific embodiment, R 1 , R 2 , R 3 and R 4 are independently -C(O)OR a ; in another specific embodiment, R 1 , R 2 , R 3 and R
- L 1 is C(R 1a )(R 2a ); in another specific embodiment, L 1 is O; in another specific embodiment, L 1 is S; in another specific embodiment, L 1 is N(R 1a ); in another specific embodiment, L 1 is C(O); in another specific embodiment, L 1 is S(O); in another specific embodiment, L 1 is S(O) 2 .
- L 2 is C(R 1b )(R 2b ); in another specific embodiment, L 2 is O; in another specific embodiment, L 2 is S; in another specific embodiment, L 2 is N(R 1b ); in another specific embodiment, L 2 is C(O); in another specific embodiment, L 2 is S(O); in another specific embodiment, L 2 is S(O) 2 .
- L 3 is C(R 1f )(R 2f ); in another specific embodiment, L 3 is O; in another specific embodiment, L 3 is S; in another specific embodiment, L 3 is N(Rif); in another specific embodiment, L 3 is C(O); in another specific embodiment, L 3 is S(O); in another specific embodiment, L 3 is S(O) 2 .
- L 4 is C(R 1g )(R 2g ); in another specific embodiment, L 4 is O; in another specific embodiment, L 4 is S; in another specific embodiment, L 4 is N(R 1g ); in another specific embodiment, L 4 is C(O); in another specific embodiment, L 4 is S(O); in another specific embodiment, L 4 is S(O) 2 .
- L 5 is C(R 1h )(R 2h ); in another specific embodiment, L 5 is O; in another specific embodiment, L 5 is S; in another specific embodiment, L 5 is N(R 1h ); in another specific embodiment, L 5 is C(O); in another specific embodiment, L 5 is S(O); in another specific embodiment, L 5 is S(O) 2 .
- X is O; in another specific embodiment, X is S; in another specific embodiment, X is N(R 1c ); in another specific embodiment, X is C(R 1c )(R 2c ).
- Y is O; in another specific embodiment, Y is S; in another specific embodiment, Y is N(R 1d ); in another specific embodiment, Y is C(R 1d )(R 2d ).
- W is O; in another specific embodiment, W is S; in another specific embodiment, W is N(R 1e ); in another specific embodiment, W is C(R 1e )(R 2e ).
- R is H; in another specific embodiment, R is C 1-6 alkyl; in another specific embodiment, R is C 1-6 haloalkyl; in another specific embodiment, R is C 3-7 cycloalkyl; in another specific embodiment, R is 3- to 7-membered heterocyclyl; in another specific embodiment, R is C 6-10 aryl; in another specific embodiment, R is 5- to 10-membered heteroaryl.
- m is 1; in another specific embodiment, m is 2; in another specific embodiment, m is 3; in another specific embodiment, m is 4; in another specific embodiment, m is 5.
- n is 1; in another specific embodiment, n is 2; in another specific embodiment, n is 3.
- R 1a and R 2a /R 1b and R 2b /R 1c and R 2c /R 1d and R 2d /R 1e and R 2e /R 1f and R 2f /R 1g and R 2g /R 1h and R 2h are independently H; in another specific embodiment, R 1a and R 2a/ R 1b and R 2b /R 1c and R 2c /R 1d and R 2d /R 1e and R 2e /R 1f and R 2f /R 1g and R 2g /R 1h and R 2h are independently D; in another specific embodiment, R 1a and R 2a /R 1b and R 2b /R 1c and R 2c /R 1d and R 2d /R 1e and R 2e /R 1f and R 2f /R 1g and R 2g /R 1h and R 2h are independently halogen; in another specific embodiment, R 1a and R 2a /R 1
- Substituents on different atoms in -X-(L 1 ) m -Y- can be connected to form C 3-10 cycloalkyl, 3- to 10-membered heterocyclyl, C 6-14 aryl or 3- to 10-membered heteroaryl.
- substituents on different atoms in -X-(L 1 ) m -Y- can be connected to form C 3-10 cycloalkyl; in another specific embodiment, substituents on different atoms in -X-(Li)mY- can be connected to form 3- to 10-membered heterocyclyl; in another specific embodiment, substituents on different atoms in -X-(L 1 ) m -Y- can be connected to form C 6-14 aryl; in another specific embodiment, substituents on different atoms in -X-(L 1 ) m -Y- can be connected to form 3- to 10-membered heteroaryl.
- Substituents on different atoms in -(L 2 ) n -W- can be connected to form C 3-10 cycloalkyl, 3- to 10-membered heterocyclyl, C 6-14 aryl or 3- to 10-membered heteroaryl.
- substituents on different atoms in -(L 2 ) n -W- can be connected to form C 3-10 cycloalkyl; in another specific embodiment, substituents on different atoms in -(L 2 ) n -W- can be connected to form 3- to 10-membered heterocyclyl; in another specific embodiment, substituents on different atoms in -(L 2 ) n -W- can be connected to form C 6-14 aryl; in another specific embodiment, substituents on different atoms in -(L 2 ) n -W- can be connected to form 3-to 10-membered heteroaryl.
- Substituents on different atoms in -L 5 -(L 3 ) n -L 4 - can be connected to form C 3-10 cycloalkyl, 3- to 10-membered heterocyclyl, C 6-14 aryl or 3- to 10-membered heteroaryl.
- substituents on different atoms in -L 5 -(L 3 ) n -L 4 - can be connected to form C 3-10 cycloalkyl; in another specific embodiment, substituents on different atoms in -L 5 -(L 3 ) n -L 4 - can be connected to form 3- to 10-membered heterocyclyl; in another specific embodiment, substituents on different atoms in -L 5 -(L 3 ) n -L 4 - can be connected to form C 6-14 aryl; in another specific embodiment, substituents on different atoms in -L 5 -(L 3 ) n -L 4 - can be connected to form 3- to 10-membered heteroaryl.
- R 1c or R 2c on the first carbon atom can form a ring with R 1a or R 2a on the second carbon atom, or R 1c or R 2c on the first carbon atom can form a ring with R 1d or R 2d on the third carbon atom, or R 1a or R 2a on the second carbon atom can form a ring with R 1d or R 2d on the third carbon atom.
- R 1b or R 2b on the first carbon atom can form a ring with R 1b or R 2b on the second carbon atom, or R 1b or R 2b on the first carbon atom can form a ring with R 1e on the third nitrogen atom, or R 1b or R 2b on the second carbon atom can form a ring with R 1e on the third nitrogen atom.
- any technical solution or any combination thereof of the above specific embodiments can be combined with any technical solution or any combination thereof of other specific embodiments.
- any technical solution or any combination thereof of A 1 can be combined with any technical solution or any combination thereof of A 1 -A 4 , R 1 -R 4 , X, Y, W, R, L 1 -L 5 , m and n.
- the present disclosure is intended to include a combination of all these technical solutions, limited to space, these technical solutions will not be listed one by one.
- the compound of the present disclosure may be selected from the following compounds: or pharmaceutically acceptable salts, enantiomers, diastereomers, racemates, solvates, hydrates, or polymorphs thereof.
- the compounds of the present disclosure may include one or more asymmetric centers, and thus may exist in a variety of stereoisomeric forms, for example, enantiomers and/or diastereomers.
- the compounds of the present disclosure may be in the form of an individual enantiomer, diastereomer or geometric isomer (e.g., cis- and trans-isomers), or may be in the form of a mixture of stereoisomers, including racemic mixture and a mixture enriched in one or more stereoisomers.
- the isomers can be separated from the mixture by the methods known to those skilled in the art, including chiral high pressure liquid chromatography (HPLC) and the formation and crystallization of chiral salts; or preferred isomers can be prepared by asymmetric synthesis.
- HPLC high pressure liquid chromatography
- organic compounds can form complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as "solvates.” Where the solvent is water, the complex is known as "hydrate.”
- solvates Where the solvent is water, the complex is known as "hydrate.”
- present disclosure encompasses all solvates of the compounds of the present disclosure.
- solvate refers to forms of a compound or a salt thereof, which are associated with a solvent, usually by a solvolysis reaction. This physical association may include hydrogen bonding.
- solvents include water, methanol, ethanol, acetic acid, DMSO, THF, diethyl ether, etc.
- Suitable solvates include pharmaceutically acceptable solvates and further include both stoichiometric solvates and non-stoichiometric solvates. In some cases, the solvates will be capable of isolation, for example, when one or more solvent molecules are incorporated into the crystal lattice of a crystalline solid.
- “Solvate” includes both solution-phase and isolatable solvates. Representative solvates include hydrates, ethanolates and methanolates.
- hydrate refers to a compound that is associated with water. Generally, the number of water molecules contained in a hydrate of a compound is in a definite ratio to the number of the compound molecules in the hydrate. Therefore, hydrates of a compound can be represented, for example, by a general formula R ⁇ x H 2 O, wherein R is the compound, and x is a number greater than 0.
- Given compounds can form more than one type of hydrates, including, for example, monohydrates (x is 1), lower hydrates (x is a number greater than 0 and smaller than 1, for example, hemihydrates (R ⁇ 0.5 H 2 O)) and polyhydrates (x is a number greater than 1, for example, dihydrates (R ⁇ 2 H 2 O) and hexahydrates (R ⁇ 6 H 2 O)).
- monohydrates x is 1
- lower hydrates x is a number greater than 0 and smaller than 1, for example, hemihydrates (R ⁇ 0.5 H 2 O)
- polyhydrates x is a number greater than 1, for example, dihydrates (R ⁇ 2 H 2 O) and hexahydrates (R ⁇ 6 H 2 O)
- polymorph refers to a crystalline form of a compound (or a salt, hydrate or solvate thereof) in a particular crystal packing arrangement. All polymorphs have the same elemental composition. Different crystalline forms generally have different X-ray diffraction patterns, infrared spectra, melting points, density, hardness, crystal shapes, optical and electrical properties, stability, and solubility. Recrystallization solvents, rate of crystallization, storage temperatures, and other factors may cause one crystalline form to dominate.
- Various polymorphs of a compound can be prepared by crystallization under different conditions.
- the present disclosure also comprises compounds that are labeled with isotopes, which are equivalent to those described in formula (I), but one or more atoms are replaced by atoms having an atom mass or mass number that are different from that of atoms that are common in nature.
- isotopes which may be introduced into the compounds of the disclosure include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine and chlorine, such as 2 H, 3 H, 13 C, 11 C, 14 C, 15 N, 18 O, 17 O, 31 P, 32 P, 35 S, 18 F and 36 Cl, respectively.
- Compounds of the present disclosure that comprise the above isotopes and/or other isotopes of other atoms, prodrugs thereof and pharmaceutically acceptable salts of said compounds or prodrugs all are within the scope of the present disclosure.
- Certain isotope-labeled compounds of the present disclosure such as those incorporating radioactive isotopes (e.g., 3 H and 14 C), can be used for the measurement of the distribution of drug and/or substrate in tissue.
- Tritium which is 3 H and carbon-14, which is 14 C isotope, are particularly preferred, because they are easy to prepare and detect.
- Isotope-labeled compounds of formula (I) of the present disclosure and prodrugs thereof can be prepared generally by using readily available isotope-labeled reagents to replace non-isotope-labeled reagents in the following schemes and/or the procedures disclosed in the examples and preparation examples.
- compositions, formulations and kits are provided.
- the disclosure provides a pharmaceutical composition
- a pharmaceutical composition comprising a compound of the present disclosure (also referred to as the "active ingredient") and a pharmaceutically acceptable excipient.
- the pharmaceutical composition comprises an effective amount of the active ingredient.
- the pharmaceutical composition comprises a therapeutically effective amount of the active ingredient.
- the pharmaceutical composition comprises a prophylactically effective amount of the active ingredient.
- a pharmaceutically acceptable excipient for use in the present disclosure refers to a non-toxic carrier, adjuvant or vehicle which does not destroy the pharmacological activity of the compound formulated together.
- Pharmaceutically acceptable carriers, adjuvants, or vehicles that may be used in the compositions of the present disclosure include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins (e.g., human serum albumin), buffer substances (such as phosphate), glycine, sorbic acid, potassium sorbate, a mixture of partial glycerides of saturated plant fatty acids, water, salt or electrolyte (such as protamine sulfate), disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salt, silica gel, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based materials, polyethylene glycol, sodium carboxymethyl cellulose, polyacrylate, wax, polyethylene-polyoxypropylene block polymers
- kits e.g., pharmaceutical packs.
- Kits provided may include a compound disclosed herein, other therapeutic agents, and a first and a second containers (e.g., vials, ampoules, bottles, syringes, and/or dispersible packages or other materials) containing the compound disclosed herein or other therapeutic agents.
- kits provided can also optionally include a third container containing a pharmaceutically acceptable excipient for diluting or suspending the compound disclosed herein and/or other therapeutic agent.
- the compound disclosed herein provided in the first container and the other therapeutic agents provided in the second container is combined to form a unit dosage form.
- parenteral administration as used herein includes subcutaneous administration, intradermal administration, intravenous administration, intramuscular administration, intra-articular administration, intraarterial administration, intrasynovial administration, intrasternal administration, intracerebroventricular administration, intralesional administration, and intracranial injection or infusion techniques.
- the compounds provided herein are administered in an effective amount.
- the amount of the compound actually administered will typically be determined by a physician, in the light of the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.
- the compounds provided herein When used to prevent the disorder disclosed herein, the compounds provided herein will be administered to a subject at risk for developing the condition, typically on the advice and under the supervision of a physician, at the dosage levels described above.
- Subjects at risk for developing a particular condition generally include those that have a family history of the condition, or those who have been identified by genetic testing or screening to be particularly susceptible to developing the condition.
- the pharmaceutical compositions provided herein can also be administered chronically ("chronic administration").
- Chronic administration refers to administration of a compound or pharmaceutical composition thereof over an extended period of time, e.g., for example, over 3 months, 6 months, 1 year, 2 years, 3 years, 5 years, etc, or may be continued indefinitely, for example, for the rest of the subject's life.
- the chronic administration is intended to provide a constant level of the compound in the blood, e.g., within the therapeutic window over the extended period of time.
- the pharmaceutical compositions of the present disclosure may be further delivered using a variety of dosing methods.
- the pharmaceutical composition may be given as a bolus, e.g., in order to raise the concentration of the compound in the blood to an effective level rapidly.
- the placement of the bolus dose depends on the desired systemic levels of the active ingredient, e.g., an intramuscular or subcutaneous bolus dose allows a slow release of the active ingredient, while a bolus delivered directly to the veins ( e.g., through an IV drip) allows a much faster delivery which quickly raises the concentration of the active ingredient in the blood to an effective level.
- the pharmaceutical composition may be administered as a continuous infusion, e.g., by IV drip, to provide maintenance of a steady-state concentration of the active ingredient in the subject's body.
- the pharmaceutical composition may be administered as first as a bolus dose, followed by continuous infusion.
- compositions for oral administration can take the form of bulk liquid solutions or suspensions, or bulk powders. More commonly, however, the compositions are presented in unit dosage forms to facilitate accurate dosing.
- unit dosage forms refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient.
- Typical unit dosage forms include prefilled, premeasured ampules or syringes of the liquid compositions or pills, tablets, capsules or the like in the case of solid compositions.
- the compound is usually a minor component (from about 0.1 to about 50% by weight or alternatively from about 1 to about 40% by weight) with the remainder being various vehicles or excipients and processing aids helpful for forming the desired dosing form.
- each dose provides from about 0.01 to about 20 mg/kg of the compound provided herein, with preferred doses each providing from about 0.1 to about 10 mg/kg, and especially about 1 to about 5 mg/kg.
- Transdermal doses are generally selected to provide similar or lower blood levels than are achieved using injection doses, generally in an amount ranging from about 0.01 to about 20% by weight, alternatively from about 0.1 to about 20% by weight, alternatively from about 0.1 to about 10% by weight, and yet alternatively from about 0.5 to about 15% by weight.
- Injection dose levels range from about 0.1 mg/kg/hour to at least 10 mg/kg/hour, all for from about 1 to about 120 hours and especially 24 to 96 hours.
- a preloading bolus of from about 0.1 mg/kg to about 10 mg/kg or more may also be administered to achieve adequate steady state levels.
- the maximum total dose is not expected to exceed about 2 g/day for a 40 to 80 kg human patient.
- Liquid forms suitable for oral administration may include a suitable aqueous or nonaqueous vehicle with buffers, suspending and dispensing agents, colorants, flavors and the like.
- Solid forms may include, for example, any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
- a binder such as microcrystalline cellulose, gum tragacanth or gelatin
- an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch
- Injectable compositions are typically based upon injectable sterile saline or phosphate-buffered saline or other injectable excipients known in the art.
- the active compound in such compositions is typically a minor component, often being from about 0.05 to 10% by weight with the remainder being the injectable excipient and the like.
- Transdermal compositions are typically formulated as a topical ointment or cream containing the active ingredient(s).
- the active ingredients When formulated as a ointment, the active ingredients will typically be combined with either a paraffinic or a water-miscible ointment base. Alternatively, the active ingredients may be formulated in a cream with, for example an oil-in-water cream base.
- Such transdermal formulations are well-known in the art and generally include additional ingredients to enhance the dermal penetration of stability of the active ingredients or Formulation. All such known transdermal formulations and ingredients are included within the scope provided herein.
- transdermal administration may be accomplished using a patch either of the reservoir or porous membrane type, or of a solid matrix variety.
- the compounds of the present disclosure can also be administered in sustained release forms or from sustained release drug delivery systems.
- sustained release materials may be found in Remington's Pharmaceutical Sciences .
- the present disclosure also relates to the pharmaceutically acceptable formulations of a compound of the present disclosure.
- the formulation comprises water.
- the formulation comprises a cyclodextrin derivative.
- the most common cyclodextrins are ⁇ -, ⁇ - and ⁇ - cyclodextrins consisting of 6, 7 and 8 ⁇ -l,4-linked glucose units, respectively, optionally comprising one or more substituents on the linked sugar moieties, which include, but are not limited to, methylated, hydroxyalkylated, acylated, and sulfoalkylether substitution.
- the cyclodextrin is a sulfoalkyl ether ⁇ -cyclodextrin, e.g., for example, sulfobutyl ether ⁇ -cyclodextrin, also known as Captisol. See, e.g., U.S. 5,376,645 .
- the formulation comprises hexapropyl- ⁇ -cyclodextrin (e.g., 10-50% in water).
- Exemplary diseases include cancer, pain, neurological diseases, autoimmune diseases, and inflammation.
- Cancers include, for example, lung cancer, colon cancer, breast cancer, prostate cancer, hepatocellular carcinoma, renal cell carcinoma, gastric and esophageal cancer, glioblastoma, head and neck cancer, inflammatory myofibroblastic tumor and anaplastic large cell lymphoma.
- Pain includes, for example, pain of any source or cause, including cancer pain, chemotherapy pain, nerve pain, injury pain or pain from other sources.
- Autoimmune diseases include, for example, rheumatoid arthritis, Sjogren syndrome, type I diabetes and lupus.
- Exemplary neurological diseases include Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and Huntington's disease.
- Exemplary inflammatory diseases include atherosclerosis, allergies, and inflammation due to infection or injury.
- the compounds and pharmaceutical compositions of the present disclosure specifically target tyrosine receptor kinases, especially ALK, ROS1 and TRK Therefore, the compounds and pharmaceutical compositions can be used to prevent, reverse, alleviate or inhibit the activity of one or more of the kinases.
- the method of treatment targets cancer. In other embodiments, the method is used to treat lung cancer or non-small cell lung cancer.
- the inhibition method of the present disclosure is intended to mean an amount effective to inhibit the target protein.
- the measurement and adjustment of targets can be implemented by conventional analytical methods (such as those described below). The adjustment can be used in a variety of settings, including in vitro analysis.
- the cells are preferably cancer cells with abnormal signal transduction due to the up-regulation of ALK, ROS1 and TRK
- effective amount is intended to refer to an amount or dosage sufficient to produce the desired therapeutic benefit in an individual in need of the treatment.
- the effective amount or dosage of the compounds of the present disclosure can be determined by conventional methods (e.g., modeling, dose escalation or clinical trials) and conventional factors (e.g., the mode or route of drug delivery, the pharmacokinetics of the drug, the severity and process of the infection, the individual's health and weight, and the judgment of the attending physician).
- Exemplary dosages are in the range of about 0.1 mg to 1 g per day, or about 1 mg to 50 mg per day, or about 50 mg to 250 mg per day or about 250 mg to 1 g per day.
- the total dosage can be in a single or separated dose units (e.g., BID, TID, QID).
- the dosage can be adjusted for preventive or maintenance treatment.
- the dosage or frequency of administration or both can be reduced according to symptoms to an amount of maintaining the required therapeutic or preventive effect.
- the treatment can be stopped.
- patients may require long-term intermittent treatment. Patients may also require long-term chronic treatment.
- the compounds described herein can be used in combination with one or more other active ingredients in pharmaceutical compositions or methods to treat the diseases and disorders described herein.
- Other additional active ingredients include other therapeutic agents or drugs that alleviate the adverse effects of the therapeutic agent on the expected disease target.
- the combination can be used to increase efficacy, improve symptoms of other diseases, reduce one or more negative effects, or reduce the required dosage of the compound of the present disclosure.
- Additional active ingredients can be formulated into a pharmaceutical composition separated from that of the compounds of the present disclosure or can be included in a single pharmaceutical composition with the compounds of the present disclosure.
- the additional active ingredient can be administered simultaneously with, before or after the administration of the compound of the present disclosure.
- Combination agents include those additional active ingredients that known or observed to be effective in the treatment of the diseases and conditions described herein, including those effectively against another target related to the disease.
- the compositions and formulations of the present disclosure, and treatment methods may further include other drugs or medicines, such as other active agents that can be used to treat or alleviate the target disease or related symptoms or conditions.
- kinase inhibitors for example, EGFR inhibitors (such as erlotinib, gefitinib); Raf inhibitors (such as vemurafenib), VEGFR inhibitors (such as sunitinib); standard chemotherapeutic agents such as alkylating agents, antimetabolites, antitumor antibiotics, topoisomerase inhibitors, platinum drugs, mitotic inhibitors, antibodies, hormone therapy or corticosteroids.
- suitable combination agents include anti-inflammatory agents, such as NSAID.
- the pharmaceutical composition of the present disclosure may additionally include one or more of the active agents, and the method of treatment may additionally include administering an effective amount of one or more of the active agents.
- each reaction is carried out in an inert solvent at a temperature from room temperature to reflux temperature (such as 0 °C to 100 °C, alternatively 0 °C to 80 °C).
- the reaction time is usually 0.1-60 hours, alternatively 0.5-24 hours.
- Example 1 Preparation of (13 R )-11-fluoro-13-methyl-6,7,13,14-tetrahydro-1,15-ethenopyrazolo[4,3- f ] [1,4,8,10]benzoxatriazacyclotridecin-5(6 H )-one (Compound T-1).
- Example 2-1 Preparation of (7S,13R)-11-fluoro-7,13-dimethyl-6,7,13,14-tetrahydro-1,15-ethenopyrazolo[4,3-f][1,4,8,10]benzoxatriazacyclotridecin-5(6H)-one (Compound T-2-A).
- Example 2-2 Preparation of (7S,13S)-11-fluoro-7,13-dimethyl-6,7,13,14-tetrahydro-1,15-ethenopyrazolo[4,3-f][1,4,8,10]benzoxatriazacyclotridecin-5(6H)-one (Compound T-2-B)
- Ethyl isobutyrate (2.5 g, 21.5 mmol) was added to a reaction flask, and 40 ml anhydrous tetrahydrofuran was added under nitrogen protection. The mixture was cooled to -40 °C, and LDA (lithium diisopropylamide, 11.8 ml, 23.6 mmol) was slowly added dropwise. After the addition, the reaction was gradually warmed to room temperature and stirred to react for half an hour. After cooled to -40 °C, a solution of diiodomethane (5.76 g, 21.5 mmol) in 10ml anhydrous tetrahydrofuran was slowly added.
- LDA lithium diisopropylamide, 11.8 ml, 23.6 mmol
- Example 7 Preparation of 9-fluoro-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 9a), (6 R )-9-fluoro-13-oxa-2,17,20,21,24-pentaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-1-A), and (6 S )-9-fluoro-13-oxa-2,17,20,21,24-pentaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,
- reaction solution was poured into 100 mL of saturated ammonium chloride solution and stirred for 10 min, then the reaction solution was separated by standing.
- the aqueous phase was extracted three times with 40 mL ethyl acetate.
- the organic phases were combined and washed with saturated brine, and dried over anhydrous sodium sulfate.
- the residue was filtered and concentrated, purified by column chromatography to afford 17.68 g of compound 1a as light yellow liquid. Yield: 61.1%.
- LC-MS (APCI): m/z 312.1 (M+1) + .
- racemic compound 9a was separated to afford target compound L-1-A (retention time: 20.33 min, relative amount: 43.4%) and L-1-B (retention time: 6.31 min, relative amount: 44.0%).
- Example 8 Preparation of (14S)-9-fluoro-14-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 13a), (6 R ,14 S )-9-fluoro-14-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-2-A), and (6S,14S)-9-fluoro-14-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0
- racemic compound 13a was separated to afford target compound L-2-A (retention time: 27.06 min, relative amount: 27.7%) and L-2-B (retention time: 7.02 min, relative amount: 67.8%).
- Example 9 Preparation of 9-fluoro-15,15-dimethyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 18a) (6 R )-9-fluoro-15,15-dimethyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-3-A), and (6 S )-9-fluoro-15,15-dimethyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12
- Ethyl isobutyrate (2.5 g, 21.5 mmol) was added to a reaction flask, and 40 ml anhydrous tetrahydrofuran was added under nitrogen protection. The mixture was cooled to -40 °C, and LDA (11.8 ml, 23.6 mmol) was slowly added dropwise. After the addition, the reaction was gradually warmed to room temperature and stirred for half an hour. Then it was cooled to - 40 °C, and a solution of diiodomethane (5.76 g, 21.5 mmol) in 10ml anhydrous tetrahydrofuran was slowly added dropwise. After the addition, the reaction was warmed to room temperature and reacted overnight.
- racemic compound 18a was separated to afford target compound L-3-A (retention time: 24.2 min, relative amount: 33.1%) and L-3-B (retention time: 8.34 min, relative amount: 61.0%).
- Example 10 Preparation of 9-fluoro-15-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 23a), (6 R , 15R )-9-fluoro-15-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-4-A), (6 R , 15S )-9-fluoro-15-methyl-13-oxa-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25
- 2-methyl-1,3-propanediol (2.0 g, 22.2 mmol) was dissolved in dichloromethane (30 ml), triethylamine (3.37 g, 33.3 mmol) was added under ice bath, and p-toluenesulfonyl chloride (TsCl, 4.23 g, 22.2 mmol) was added in batches while maintaining the temperature no higher than 5°C. After the addition, the reaction was stirred and reacted at the low temperature for 2-3 hours. TLC was used to monitor the completion of the reaction.
- racemic compound 23a was separated to afford target compound L-4-A (retention time: 6.28 min, relative amount: 22.3%), L-4-B (retention time: 18.46 min, relative amount: 22.4%), L-4-C (retention time: 30.45 min, relative amount: 22.2%) and L-4-D (retention time: 37.26 min, relative amount: 22.4%).
- Example 11 Preparation of 9-fluoro-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 28a), (6 R )-9-fluoro-2,17,20,21,24-pentaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-5-A), and (6 S )-9-fluoro-2,17,20,21,24-pentaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene
- racemic compound 28a was separated to afford target compound L-5-A (retention time: 6.28 min, relative amount: 44.6%) and L-5-B (retention time: 18.46 min, relative amount: 44.8%).
- Example 12 Preparation of 9-fluoro-15-methyl-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 32a), (6 R , 15R )-9-fluoro-15-methyl-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-6-A), (6R,15S)-9-fluoro-15-methyl-2,17,20,21,24-pentaazapentacyclo [16.5.2.0 2,6 .0 7,12 .0 21,25 ] pentacosane-1(24),7,9,11
- racemic compound 32a was separated to afford target compound L-6-A (retention time: 7.14 min, relative amount: 21.6%), L-6-B (retention time: 15.69 min, relative amount: 22.8%), L-6-C (retention time: 29.54 min, relative amount: 17.6%) and L-6-D (retention time: 34.26 min, relative amount: 16.9%).
- Example 13 Preparation of 9-fluoro-15-methyl-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 41a), (6 R , 15R )-9-fluoro-15-methyl-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-7-A), (6 R , 15S )-9-fluoro-15-methyl-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1
- racemic compound 41a was separated to afford target compound L-7-A (retention time: 4.77 min, relative amount: 30.21%), L-7-B (retention time: 15.68 min, relative amount: 22.5%), L-7-C (retention time: 26.31 min, relative amount: 10.66%) and L-7-D (retention time: 29.67 min, relative amount: 23.4%).
- Example 14 Preparation of 9-fluoro-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 45a), (6 R )-9-fluoro-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-8-A), and (6 S )-9-fluoro-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22
- racemic compound 45a was separated to afford target compound L-8-A (retention time: 20.15 min, relative amount: 43.7%) and L-8-B (retention time: 8.25 min, relative amount: 44.0%).
- Example 15 Preparation of (4 R )-9-fluoro-4-hydroxy-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound 56a), (4 R , 6R )-9-fluoro-4-hydroxy-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]pentacosane-1(24),7,9,11,18(25),19,22-heptaene-16-one (Compound L-9-A), and (4 R , 6S )-9-fluoro-4-hydroxy-2,11,17,20,21,24-hexaazapentacyclo[16.5.2.0 2,6 .0 7,12 .0 21,25 ]penta
- reaction solution was poured into 100 mL of saturated ammonium chloride solution and stirred for 10 min, then the reaction solution was separated by standing.
- the aqueous phase was extracted three times with 40 mL ethyl acetate.
- the organic phases were combined and washed with saturated brine, dried over anhydrous sodium sulfate.
- the residue was filtered and concentrated, purified by column chromatography to afford 18.5g of compound 48a as light yellow liquid. Yield: 61.1%.
- LC-MS(APCI): m/z 490.2(M+1) + .
- racemic compound 56a was separated to afford target compound L-9-A (retention time: 14.26 min, relative amount: 45.0%) and L-9-B (retention time: 5.38 min, relative amount: 42.9%).
- Example 16 Preparation of 9-fluoro-13-oxa-2,11,18,21,22,25-hexaazapentacyclo[17.5.2.0 2,6 .0 7,12 .0 22,26 ]hexadecane-1(25),7,9,11,19(26),20,23-heptaene-17-one (Compound 64a), ( 6 R )-9-fluoro-13-oxa-2,11,18,21,22,25-hexaazapentacyclo[17.5.2.0 2,6 .0 7,12 .0 22,26 ]hexadecane-1(25),7,9,11,19(26),20,23-heptaene-17-one (Compound L-10-A), and ( 6 S )-9-fluoro-13-oxa-2,11,18,21,22,25-hexaazapentacyclo[17.5.2.0 2,6 .0 7,12 .0 22,26 ]hexadecane-1(25
- racemic compound 64a was separated to afford target compound L-10-A (retention time: 27.54 min, relative amount: 49.4%) and L-10-B (retention time: 38.22 min, relative amount: 49.3%).
- TRKA, TRKB, TRKC kinases can be measured by HTRF (High Fluorescence Resonance Energy Transfer) method.
- the reaction was performed in a 384-well plate at 23 °C with a volume of 20 ⁇ L.
- TRKA, TRKB or TRKC kinase were mixed with pre-formulated and diluted compounds of different concentrations for ten minutes in duplicate for each concentration, wherein 11 concentrations made with a 3-fold gradient dilution from the starting concentration of 300 nM were made and the final concentration of DMSO was 2%.
- the corresponding substrate and ATP were added thereto, and reacted at room temperature for 20 minutes (both a negative and a positive control were set: negative control is blank control, positive control is Entrectinib).
- detection reagent was added thereto (reagent in HTRF Kinase TK kit), and after incubation at room temperature for 30 minutes, detection was carried out by PerkinElmer Envision microplate reader for determining enzyme activity in the presence of the compounds of the present disclosure at various concentrations, and the inhibitory activity of different concentrations of compounds against enzyme activity was calculated. After that, in accordance with four-factors function and Graphpad 5.0 software, inhibitory activity on enzyme activity under different concentrations of compounds was fitted and IC 50 values were calculated. The data of the compounds tested in this analysis is shown in Table 1.
- the CGT method was used to detect the in vitro anti-proliferative activity of the compounds of the present disclosure on tumor cells cultured in vitro.
- the KM12 cell line was maintained in RPMI-1640 medium containing 10% fetal bovine serum and antibiotics, the cells in the logarithmic growth phase were harvested and planted in a 96-well plate. The plate was incubated in an incubator at 37 °C, containing 5% carbon dioxide gas overnight. After the test compounds were dissolved in DMSO, a 3-fold concentration gradient dilution with 9 compound concentrations was made. Pre-prepared compounds of different concentrations were transferred to the cell plate in triplicate for each concentration, and continue culturing for 72 h. The final concentration of DMSO in the system was 0.1%, and the initial concentration of the test compound was 300 nM.
- the CGT method was used to detect the in vitro anti-proliferative activity of the compounds of the present disclosure on three cell lines cultured in vitro.
- the Ba/F3 parent cells, Ba/F3 LMNA-NTRK1 and Ba/F3 LMNA-NTRK1 -G595R cells were maintained in RPMI-1640 medium containing 10% fetal bovine serum and antibiotics, respectively, and the cells in the logarithmic growth phase were harvested and planted in a 96-well plate. The plate was incubated in a incubator at 37 °C, containing 5% carbon dioxide gas overnight, wherein 8 ng/ml IL-3 was added to the Ba/F3 parent cells. After dissolving the test compounds in DMSO, 9 compound concentrations were made with a 3.16-fold gradient dilution.
- the pre-prepared compounds of different concentrations were transferred to the cell plate in triplicate for each concentration, and continued for culturing for 72 h.
- the final concentration of DMSO in the system was 0.1%
- the initial concentration of the test compounds in the Ba/F3 parent cell was 10 ⁇ M
- the initial concentration of the test compounds in Ba/F3 LMNA-NTRK1 and Ba/F3 LMNA-NTRK1-G595R cells was 1 ⁇ M.
- CellTiter-Glo reagent was added to the cell plate, and incubated at room temperature for 30minutes to stabilize the optical signal. Detection was carried out by PerkinElmer Envision microplate reader for determining the inhibitory activity of the compound of the present disclosure at various concentrations on cell proliferation.
- the inhibitory activity of compounds at different concentrations on cell proliferation was fitted according to Graphpad 5.0 software, and IC 50 values were calculated. The results showed that the compound of the present disclosure has almost no inhibitory effect on Ba/F3 parent cells but has an inhibitory effect on Ba/F3 LMNA-NTRK1 and Ba/F3 LMNA-NTRK1-G595R cells.
- mice 6 male Sprague-Dawley rats (7-8 weeks old, and weighing approximately 210 g) were divided into 2 groups with 3 rats in each group.
- the rats were intravenously or orally administered a single dose of compounds (3mg/kg intravenously, 10 mg/kg orally) to compare pharmacokinetic differences.
- the rats were feeded on standard food and water. Fasting was started 16 hours before the test.
- the drug was dissolved in PEG400 and dimethyl sulfoxide.
- the blood samples were collected from eyelids at the time points of 0.083 hour, 0.25 hour, 0.5 hour, 1 hour, 2 hours, 4 hours, 6 hours, 8 hours, 12 hours, and 24 hours after administration.
- Rats were briefly anesthetized after inhalation of diethyl ether and 300 ⁇ L of blood sample was collected from the eyelids into test tubes. There was 30 ⁇ L of 1% heparin salt solution in the test tube. Tubes were dried at 60°C overnight before use. After the blood sample was collected at the last time point, the rats were sacrificed after ether anesthesia.
- the test tube was gently inverted at least 5 times to ensure sufficient mixing and then placed on ice.
- the blood sample was centrifuged at 5000 rpm at 4°C for 5 minutes to separate the plasma from the red blood cells.
- 100 ⁇ L of plasma was aspirated into a clean plastic centrifuge tube with a pipette, marking with the name of the compound and time point.
- Plasma was stored at -80°C prior to analysis.
- the concentration of the compound of the present disclosure in plasma was determined by LC-MS/MS.
- the pharmacokinetic parameters were calculated based on the blood concentration of the drug for each animal at different time points.
- Table 2 TPX-0005 T-1 T-2-A Dosage (mg/kg) IV 3 PO 10 IV 3 PO 10 IV 3 PO 10 T max (h) 0.08 1.67 0.08 1.67 0.08 2.17 C max (h) 2185.8 731.8 2120.7 1863.8 2101.3 994.4 AUC last (h ⁇ ng/mL) 3558.9 5474.1 6238.6 11543.3 6560.9 11522.3 AUC lNF_pred (h ⁇ ng/mL) 3577.6 5586.6 6348.3 13062.9 6617.6 12905.9 MRT INF_pred (h) 1.76 5.42 4.04 6.23 3.44 7.37 V Z_pred (L/kg) 4.46 15.81 3.28 10.05 2.
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- Pyridine Compounds (AREA)
Claims (14)
- Composé de formule (I) :A1 est choisi parmi CR1 ou N ;A2 est choisi parmi CR2 ou N ;A3 est choisi parmi CR3 ou N ;A4 est choisi parmi CR4 ou N ;dans lequel R1, R2, R3 et R4 sont choisis indépendamment parmi H, halogène, -CN, -NO2, -ORa, -SRa, -NRbRc, -C(O)Ra, -C(O)ORa, -C(O)NRbRc, - OC(O)Ra, -NRbC(O)Ra, -S(O)Ra, -S(O)2Ra, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;dans lequel Ra, Rb et Rc sont chacun indépendamment choisis parmi H, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;L1 est choisi parmi C(R1a)(R2a), O, S, N(R1a), C(O), S(O) ou S(O)2 ;L2 est choisi parmi C(R1b)(R2b), O, S, N(R1b), C(O), S(O) ou S(O)2 ;X est choisi parmi O, S, N(R1c) ou C(R1c)(R2c);Y est choisi parmi O, S, N(R1d) ou C(R1d)(R2d) ;W est choisi parmi O, S, N(R1e) ou C(R1e)(R2e) ;R est choisi parmi H, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;m est choisi parmi 1, 2, 3, 4 ou 5 ;n est choisi parmi 1, 2 ou 3 ;dans lequel,R1a et R2a sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1a, R2a conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1b et R2b sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1b, R2b conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1c et R2c sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1e, R2c conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1d et R2d sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1d, R2d conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1e et R2e sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1e, R2e conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;les substituants sur différents atomes dans -X-(L1)m-Y- peuvent être connectés pour former un cycloalkyle en C3-10, un hétérocyclyle à 3 à 10 chaînons, un aryle en C6-14 ou un hétéroaryle à 3 à 10 chaînons ;les substituants sur différents atomes dans -(L2)n-W- peuvent être connectés pour former un cycloalkyle en C3-10, un hétérocyclyle à 3 à 10 chaînons, un aryle en C6-14 ou un hétéroaryle à 3 à 10 chaînons ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon la revendication 1, qui est le composé de formule (III-1) ou (III-2) :A1 est choisi parmi CR1 ou N ;A4 est choisi parmi CR4 ou N ;dans lequel R1, R3 et R4 sont choisis indépendamment parmi H, halogène, - CN, -NO2, -ORa, -SRa, -NRbRc, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;dans lequel Ra, Rb et Rc sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;X est choisi parmi O ou C(R1c)(R2c) ;Y est choisi parmi N(R1d) ou C(R1d)(R2d) ;W est choisi parmi O ou NH ;m est choisi parmi 1, 2 ou 3 ;R1a et R2a sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRe, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1a, R2a conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1b est choisi parmi H, halogène, -alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, - alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ;dans lequel,R1c et R2c sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1c, R2c conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1d et R2d sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1d, R2d conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;les substituants sur différents atomes dans -X-(C(R1a)(R2a))m-Y- peuvent être connectés pour former un cycloalkyle en C3-10, un hétérocyclyle à 3 à 10 chaînons, un aryle en C6-14 ou un hétéroaryle à 3 à 10 chaînons ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon la revendication 1 ou 2, qui est le composé de formule (IV-1) ou (IV-2) :R3 est choisi parmi H, halogène, -CN, -NO2, -ORa, -SRa ou -NRbRc ;dans lequel Ra, Rb et Rc sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;X est choisi parmi O ou C(R1c)(R2c) ;Y est choisi parmi NH, CH2 ou C(Me)(Me) ;m est choisi parmi 1, 2 ou 3 ;R1a et R2a sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1a, R2a conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1b est choisi parmi H, halogène, -alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, - alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ;dans lequel, R1c et R2c sont chacun indépendamment choisis parmi H, halogène, -alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, - alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, - alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hètèroaryle à 5 à 10 chaînons ; ou R1c, R2c conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;en variante,R3 est choisi parmi H, halogène, -CN ou -NO2 ;X est O ;Y est choisi parmi NH, CH2 ou C(Me)(Me) ;m est choisi parmi 1, 2 ou 3 ;R1a et R2a sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;R1b est choisi parmi alkyle en C1-6 ou haloalkyle en C1-6 ;en variante,R3 est choisi parmi H, halogène, -CN ou -NO2 ;X est O ;Y est choisi parmi CH2 ou C(Me)(Me) ;m est choisi parmi 1, 2 ou 3 ;R1a et R2a sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;R1b est choisi parmi alkyle en C1-6 ou haloalkyle en C1-6 ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon l'une quelconque des revendications 1 à 3, qui est le composé de formule (VI-1) ou (VI-2) :R3 est choisi parmi H, halogène, -CN ou -NO2 ;R1a et R2a sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;R1b est choisi parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon la revendication 1 qui est le composé de formule (I') :A1 est choisi parmi CR1 ou N ;A2 est choisi parmi CR2 ou N ;A3 est choisi parmi CR3 ou N ;A4 est choisi parmi CR4 ou N ;dans lequel R1, R2, R3 et R4 sont choisis indépendamment parmi H, halogène, -CN, -NO2, -ORa, -SRa, -NRbRc, -C(O)Ra, -C(O)ORa, -C(O)NRbRc, - OC(O)Ra, -NRbC(O)Ra, -S(O)Ra, -S(O)2Ra, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;dans lequel Ra, Rb et Rc sont chacun indépendamment choisis parmi H, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;L1 est choisi parmi C(R1a)(R2a), O, S, N(R1a), C(O), S(O) ou S(O)2 ;X est choisi parmi O, S, N(R1c) ou C(R1c)(R2c);Y est choisi parmi O, S, N(R1d) ou C(R1d)(R2d) ;L3 est choisi parmi C(R1f)(R2f), O, S, N(R1f), C(O), S(O) ou S(O)2;L4 est choisi parmi C(R1g)(R2g), O, S, N(R1g), C(O), S(O) ou S(O)2;L5 est choisi parmi C(R1h)(R2h), O, S, N(R1h), C(O), S(O) ou S(O)2;R est choisi parmi H, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;m est choisi parmi 1, 2, 3, 4 ou 5 ;n est choisi parmi 1, 2 ou 3 ;dans lequel,R1a et R2a sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1a, R2a conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1c et R2c sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1c, R2c conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1d et R2d sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1d, R2d conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1f et R2f sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1f, R2f conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1g et R2g sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1g, R2g conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1h et R2h sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1h, R2h conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;les substituants sur différents atomes dans -X-(L1)m-Y- peuvent être connectés pour former un cycloalkyle en C3-10, un hétérocyclyle à 3 à 10 chaînons, un aryle en C6-14 ou un hétéroaryle à 3 à 10 chaînons ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon la revendication 5 qui est le composé de formule (III'-1) ou (III'-2):A1 est choisi parmi CR1 ou N ;dans lequel R1 et R3 sont chacun indépendamment choisis parmi H, halogène, -CN, -NO2, -ORa, -SRa, -NRbRc, alkyle en C1-6, haloalkyle en C1-6, cycloalkyle en C3-7, hétérocyclyle à 3 à 7 chaînons, aryle en C6-10 ou hétéroaryle à 5 à 10 chaînons ;dans lequel Ra, Rb et Rc sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;X est choisi parmi O ou C(R1c)(R2c) ;Y est choisi parmi CH2, CH(R1d) ou C(R1d)(R2d) ;R1a et R2a sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1a, R2a conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1c et R2c sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1c, R2c conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1d et R2d sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1d, R2d conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;R1f et R2f sont chacun indépendamment choisis parmi H, halogène, - alkylène en C0-6-CN, -alkylène en C0-6-ORa, -alkylène en C0-6-SRa, -alkylène en C0-6-NRbRc, -alkylène en C0-6-C(O)Ra, -alkylène en C0-6-C(O)ORa, -alkylène en C0-6-C(O)NRbRc, alkyle en C1-6, haloalkyle en C1-6, alcényle en C2-6, alcynyle en C2-6, -alkylène en C0-6-cycloalkyle en C3-6, -alkylène en C0-6-hétérocyclyle à 3 à 7 chaînons, -alkylène en C0-6-aryle en C6-10 ou -alkylène en C0-6-hétéroaryle à 5 à 10 chaînons ; ou R1f, R2f conjointement avec l'atome auquel ils sont liés forment un cycloalkyle en C3-7 ou un hétérocyclyle à 3 à 7 chaînons ;m est choisi parmi 1, 2 ou 3 ;les substituants sur différents atomes dans -X-(C(R1a)(R2a))m-Y- peuvent être connectés pour former un cycloalkyle en C3-10, un hétérocyclyle à 3 à 10 chaînons, un aryle en C6-14 ou un hétéroaryle à 3 à 10 chaînons ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composé selon la revendication 5 ou 6, qui est le composé de formule (V'-1) ou (V'-2) :R3 est choisi parmi H, halogène, -CN ou -NO2 ;R1a et R2a sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ;en variante,R3 est choisi parmi H, halogène, -CN ou -NO2 ;R1a et R2a sont chacun indépendamment choisis parmi H, alkyle en C1-6 ou haloalkyle en C1-6 ; et R1a et R2a ne sont pas H ou D en même temps ;ou leurs sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables.
- Composition pharmaceutique, comprenant un composé selon l'une quelconque des revendications 1 à 12 ou des sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables de celui-ci, et un ou des excipients pharmaceutiquement acceptables.
- Composé selon l'une quelconque des revendications 1 à 12 ou ses sels, énantiomères, diastéréoisomères, racémates, solvates, hydrates ou polymorphes pharmaceutiquement acceptables, à utiliser dans le traitement des cancers, de la douleur, des maladies neurologiques, des maladies auto-immunes et de l'inflammation.
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CN110627812B (zh) * | 2018-06-25 | 2022-10-11 | 北京诺诚健华医药科技有限公司 | 作为trk抑制剂的杂环化合物 |
CN113773335A (zh) * | 2019-06-21 | 2021-12-10 | 成都海博为药业有限公司 | 一种作为蛋白质激酶抑制剂的化合物及其制备方法和用途 |
WO2021042890A1 (fr) * | 2019-09-04 | 2021-03-11 | 罗欣药业(上海)有限公司 | Composé hétérocyclique et son application en tant qu'inhibiteur de trk kinase |
CN112979654B (zh) * | 2019-12-16 | 2024-03-19 | 赛诺哈勃药业(成都)有限公司 | 杂芳基稠环化合物、其制备方法及应用 |
CN114230553B (zh) * | 2020-09-09 | 2023-05-05 | 凯特立斯(深圳)科技有限公司 | 一种左旋烟碱的不对称合成方法 |
CN114907315B (zh) * | 2022-05-17 | 2023-09-12 | 重庆医科大学 | Selitrectinib中间体的合成方法 |
CN115746023B (zh) * | 2022-10-27 | 2024-08-09 | 复旦大学 | 一种作为蛋白激酶抑制剂的含吲唑结构的杂环大环化合物及其制备方法 |
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US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
LT3205654T (lt) * | 2010-05-20 | 2019-05-27 | Array Biopharma, Inc. | Makrocikliniai junginiai kaip trk kinazės slopikliai |
AU2014230485A1 (en) | 2013-03-15 | 2015-09-24 | Oncodesign S.A. | Macrocyclic LRRK2 kinase inhibitors |
KR20150133765A (ko) | 2013-03-15 | 2015-11-30 | 온코디자인 에스.에이. | 거대고리 rip2 키나제 억제제 |
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PT3319969T (pt) * | 2015-07-06 | 2024-06-17 | Turning Point Therapeutics Inc | Polimorfo de macrociclo de diarilo |
RU2020123800A (ru) | 2015-07-21 | 2020-10-02 | Тёрнинг Поинт Терапьютикс, Инк. | Хиральные диарильные макроциклы и их применение |
EP3368039A1 (fr) * | 2015-10-26 | 2018-09-05 | The Regents of The University of Colorado, A Body Corporate | Mutations ponctuelles dans le cancer résistant aux inhibiteurs de trk et méthodes associées |
WO2017148325A1 (fr) * | 2016-03-03 | 2017-09-08 | 深圳市塔吉瑞生物医药有限公司 | Macrocycle et composition comprenant le macrocycle |
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TW201932472A (zh) * | 2018-01-30 | 2019-08-16 | 大陸商上海吉倍生物技術有限公司 | 具有大環分子結構的化合物及其用途 |
CN110156813B (zh) * | 2018-02-13 | 2023-07-25 | 北京诺诚健华医药科技有限公司 | 作为trk抑制剂的杂环化合物 |
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CN113956269A (zh) | 2022-01-21 |
EP3770161A4 (fr) | 2021-04-28 |
CN110386944A (zh) | 2019-10-29 |
JP7092405B2 (ja) | 2022-06-28 |
JP2021521239A (ja) | 2021-08-26 |
US11358973B2 (en) | 2022-06-14 |
CN110386944B (zh) | 2021-10-29 |
WO2019201131A1 (fr) | 2019-10-24 |
US20210171542A1 (en) | 2021-06-10 |
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